Low-memory and high-performance architectures for the CCSDS 122.0-B-1 compression standard

Two low-memory and high-performance architectures for the CCSDS 122.0-B-1 standard are proposed. They use novel memory organizations to reduce the total memory requirements in order to be implemented in a single FPGA device. The architectures were implemented in radiation-hardened and commercial FPGA devices. Based on the experimental results for the case of Virtex5QV radiation-hardened device, the throughput is 135 MSamples/sec for image with 12 bits/pixel and horizontal resolution up 8192 pixels. Also, the proposed architectures outperform the existing one in terms of the memory requirements and area.     

1-甲基环丙烯结合不同保鲜袋对叶用甘薯茎尖冷藏保鲜效果的影响

目的探究1-甲基环丙烯(1-methylcyclopropylene,1-MCP)结合不同保鲜袋对叶用甘薯茎尖贮藏品质的影响,筛选最适的保鲜方式。方法以叶用甘薯茎尖为材料,经0.91μL/L1-MCP处理24h后结合聚乙烯(PE)或微孔膜(WK)保鲜袋包装,在5℃下进行贮藏,分别于0、3、6、9、12 d时对其失重率、色差、黄化率、呼吸强度、乙烯释放量、多酚氧化酶活性等指标进行测定。结果贮藏12 d后, 1-MCP+PE, 1-MCP+WK处理组的失重率分别为3.43%,2.72%,显著低于未经1-MCP处理组(P0.05),说明1-MCP处理能够有效抑制叶用甘薯茎尖失水; 1-MCP+WK处理下的L值为33.9,高于其余3种处理,表明该处理能够更好的保持叶用甘薯茎尖的亮度和新鲜感。此外,1-MCP结合保鲜袋处理能够减弱呼吸作用,降低乙烯释放量及多酚氧化酶活性。结论1-MCP处理并结合PE膜或者微孔膜包装对叶用甘薯茎尖具有良好的保鲜效果,可以有效延长其贮藏期。     

Dhh1 is a member of the SESA network

The correct separation of chromosomes during mitosis is necessary to prevent genetic instability and aneuploidy, which are responsible for cancer and other diseases, and it depends on proper centrosome duplication. In a recent study, we found that Smy2 can suppress the essential role of Mps2 in the insertion of yeast centrosome into the nuclear membrane by interacting with Eap1, Scp160, and Asc1 and designated this network as SESA (S my2, E ap1, S cp160, A sc1). Detailed analysis showed that the SESA network is part of a mechanism which regulates translation of POM34 mRNA. Thus, SESA is a system that suppresses spindle pole body duplication defects by repressing the translation of POM34 mRNA. In this study, we performed a genome-wide screening in order to identify new members of the SESA network and confirmed Dhh1 as a putative member. Dhh1 is a cytoplasmic DEAD-box helicase known to regulate translation. Therefore, we hypothesized that Dhh1 is responsible for the highly selective inhibition of POM34 mRNA by SESA.     

Effects of hydrogen enhancement on mesoscale burner array flame stability under acoustic perturbations

Partial substitution of hydrocarbon fuel with hydrogen can effectively improve small-scale combustion system stability and performance, potentially opening the way for novel compact power generation and/or propulsion systems in the future. In this study, the effects of hydrogen enhancement between 0% and 40% hydrogen volumetric fractions in methane fuel were experimentally observed in a mesoscale burner array subjected to external acoustic perturbations. The mesoscale burner array utilizes an array of swirl-stabilized burner elements and their interactions with neighboring elements to improve the overall flame stability and simultaneously reduces the combustor length scale. OH1 chemiluminescence and OH planar laser-induced fluorescence (OH-PLIF) were used to image various hydrogen-enriched flames at an equivalence ratio of 0.7, subjected to transverse acoustic perturbations at 320 Hz. Two acoustic modes were imposed by controlling the phase difference between two speakers perturbing the flow. OH1 chemiluminescence images exhibited flame length scale reduction, leading to a denser flame array. Also, flame arrays with higher hydrogen enrichment were found to be more robust against transverse acoustic perturbations, demonstrated by reduced fluctuations in the global heat release rate. OH-PLIF images showed that flames with higher hydrogen enrichment initiated V- to M-shaped flame shape transition even under fuel lean conditions, thereby improving the combustion stability. OH-PLIF images were also used for flame stability analysis through spectral proper orthogonal decomposition (SPOD). The SPOD analysis showed hydrogen enrichment diminished flame fluctuation structures under fuel lean operation.     

Dielectric,ferroelectric, and piezoelectric properties of lead-free Ba0.95Ca0.05Ti1-xZrxO3 ceramics

Abstract

Ba_0.95Ca_0.05Ti_1-xZr_xO₃ (BCTZO) ceramics were prepared by a solid state reaction method. The samples were characterized by X-ray diffraction (XRD), Scanning electron microscopy (SEM) and X-ray absorption near edge structure (XANES). The ceramics exhibit a pure perovskite structure. The average grain size gradually decreases with increasing Zr concentration. XANES results indicate that the intensities of pre-edge peaks dropped with increasing Zr concentration. The BCTZO ceramic of x?=?0.05 has the optimum electrical properties with the maximum dielectric constant (ε'_m), remanent polarization (2P_r), coercive electric field (2E_c) and piezoelectric charge constant (d₃₃) of 7,244, 12.54 (μC/cm²), 5.29 (kV/cm) and 288 (pC/N), respectively.     

The Interfacial Interactions of Glycine and Short Glycine Peptides in Model Membrane Systems

The interactions of amino acids and peptides at model membrane interfaces have considerable implications for biological functions, with the ability to act as chemical messengers, hormones, neurotransmitters, and even as antibiotics and anticancer agents. In this study, glycine and the short glycine peptides diglycine, triglycine, and tetraglycine are studied with regards to their interactions at the model membrane interface of Aerosol-OT (AOT) reverse micelles via ¹H NMR spectroscopy, dynamic light scattering (DLS), and Langmuir trough measurements. It was found that with the exception of monomeric glycine, the peptides prefer to associate between the interface and bulk water pool of the reverse micelle. Monomeric glycine, however, resides with the N-terminus in the ordered interstitial water (stern layer) and the C-terminus located in the bulk water pool of the reverse micelle.     

The Bark Beetle Dendroctonus rhizophagus (Curculionidae: Scolytinae) Has Digestive Capacity to Degrade Complex Substrates: Functional Characterization and Heterologous Expression of an α-Amylase

Dendroctonus-bark beetles are natural agents contributing to vital processes in coniferous forests, such as regeneration, succession, and material recycling, as they colonize and kill damaged, stressed, or old pine trees. These beetles spend most of their life cycle under stem and roots bark where they breed, develop, and feed on phloem. This tissue is rich in essential nutrients and complex molecules such as starch, cellulose, hemicellulose, and lignin, which apparently are not available for these beetles. We evaluated the digestive capacity of Dendroctonus rhizophagus to hydrolyze starch. Our aim was to identify α-amylases and characterize them both molecularly and biochemically. The findings showed that D. rhizophagus has an α-amylase gene (AmyDr) with a single isoform, and ORF of 1452 bp encoding a 483-amino acid protein (53.15 kDa) with a predicted signal peptide of 16 amino acids. AmyDr has a mutation in the chlorine-binding site, present in other phytophagous insects and in a marine bacterium. Docking analysis showed that AmyDr presents a higher binding affinity to amylopectin compared to amylose, and an affinity binding equally stable to calcium, chlorine, and nitrate ions. AmyDr native protein showed amylolytic activity in the head-pronotum and gut, and its recombinant protein, a polypeptide of ~53 kDa, showed conformational stability, and its activity is maintained both in the presence and absence of chlorine and nitrate ions. The AmyDr gene showed a differential expression significantly higher in the gut than the head-pronotum, indicating that starch hydrolysis occurs mainly in the midgut. An overview of the AmyDr gene expression suggests that the amylolytic activity is regulated through the developmental stages of this bark beetle and associated with starch availability in the host tree.     

Targeting S1PRs as a Therapeutic Strategy for Inflammatory Bone Loss Diseases—Beyond Regulating S1P Signaling

As G protein coupled receptors, sphingosine-1-phosphate receptors (S1PRs) have recently gained attention for their role in modulating inflammatory bone loss diseases. Notably, in murine studies inhibiting S1PR2 by its specific inhibitor, JTE013, alleviated osteoporosis induced by RANKL and attenuated periodontal alveolar bone loss induced by oral bacterial inflammation. Treatment with a multiple S1PRs modulator, FTY720, also suppressed ovariectomy-induced osteoporosis, collagen or adjuvant-induced arthritis, and apical periodontitis in mice. However, most previous studies and reviews have focused mainly on how S1PRs manipulate S1P signaling pathways, subsequently affecting various diseases. In this review, we summarize the underlying mechanisms associated with JTE013 and FTY720 in modulating inflammatory cytokine release, cell chemotaxis, and osteoclastogenesis, subsequently influencing inflammatory bone loss diseases. Studies from our group and from other labs indicate that S1PRs not only control S1P signaling, they also regulate signaling pathways induced by other stimuli, including bacteria, lipopolysaccharide (LPS), bile acid, receptor activator of nuclear factor κB ligand (RANKL), IL-6, and vitamin D. JTE013 and FTY720 alleviate inflammatory bone loss by decreasing the production of inflammatory cytokines and chemokines, reducing chemotaxis of inflammatory cells from blood circulation to bone and soft tissues, and suppressing RANKL-induced osteoclast formation.     

Neuroprotective and Anti-Inflammatory Effects of Evernic Acid in an MPTP-Induced Parkinson’s Disease Model

Oxidative stress, mitochondrial dysfunction, and neuroinflammation are strongly associated with the pathogenesis of Parkinson’s disease (PD), which suggests that anti-oxidative and anti-inflammatory compounds might provide an alternative treatment for PD. Here, we evaluated the neuroprotective effects of evernic aid (EA), which was screened from a lichen library provided by the Korean Lichen Research Institute at Sunchon National University. EA is a secondary metabolite generated by lichens, including Ramalina, Evernia, and Hypogymnia, and several studies have described its anticancer, antifungal, and antimicrobial effects. However, the neuroprotective effects of EA have not been studied. We found that EA protected primary cultured neurons against 1-methyl-4-phenylpyridium (MPP⁺)-induced cell death, mitochondrial dysfunction, and oxidative stress, and effectively reduced MPP⁺-induced astroglial activation by inhibiting the NF-κB pathway. In vivo, EA ameliorated MPTP-induced motor dysfunction, dopaminergic neuronal loss, and neuroinflammation in the nigrostriatal pathway in C57BL/6 mice. Taken together, our findings demonstrate that EA has neuroprotective and anti-inflammatory effects in PD models and suggest that EA is a potential therapeutic candidate for PD.